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Metabolism of Isoprenaline in Dog and Man

Overview
Journal Br J Pharmacol
Publisher Wiley
Specialty Pharmacology
Date 1972 Nov 1
PMID 4656607
Citations 26
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Abstract

1. The metabolism of isoprenaline has been studied in man and dog following intravenous and oral or intra-duodenal administration.2. Intravenous isoprenaline was excreted largely unchanged in urine in both species. Only one-third of the radioactivity in urine was in the form of the O-methyl metabolite.3. After oral doses in man or intraduodenal doses in dogs, plasma radioactivity was almost entirely as conjugated isoprenaline and this metabolite accounted for more than 80% of radioactivity in urine.4. Catechol-O-methyl transferase may be less important than Uptake(2) in limiting the pharmacological action of isoprenaline.5. Pharmacological response (heart-rate increase) was related to plasma concentration of isoprenaline only after rapid intravenous injections. In dogs, following prolonged infusion or intraduodenal doses, heart rate returned to base-line values when plasma concentrations of isoprenaline were high.

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References
1.
Conolly M, Davies D, Dollery C, George C . Resistance to -adrenoceptor stimulants (a possible explanation for the rise in ashtma deaths). Br J Pharmacol. 1971; 43(2):389-402. PMC: 1665912. View

2.
CONWAY W, MINATOYA H, LANDS A, SHEKOSKY J . Absorption and elimination profile of isoproterenol. 3. The metabolic fate of dl-isoproterenol-7-3H in the dog. J Pharm Sci. 1968; 57(7):1135-41. DOI: 10.1002/jps.2600570710. View

3.
Emons E, Conolly M . Digital heart rate meter. Cardiovasc Res. 1971; 5(1):157-60. DOI: 10.1093/cvr/5.1.157. View

4.
Speizer F, DOLL R, Heaf P, Strang L . Investigation into use of drugs preceding death from asthma. Br Med J. 1968; 1(5588):339-43. PMC: 1984849. DOI: 10.1136/bmj.1.5588.339. View

5.
Axelrod J . Methylation reactions in the formation and metabolism of catecholamines and other biogenic amines. Pharmacol Rev. 1966; 18(1):95-113. View